Bioactivity of Samsum ant (<it>Pachycondyla sennaarensis</it>) venom against lipopolysaccharides through antioxidant and upregulation of Akt1 signaling in rats
<p>Abstract</p> <p>Background</p> <p>This study aimed at investigating the oxidative stress ameliorating effect, lipids profile restoration, and the anti-inflammatory effect of Samsum Ant Venom (SAV) in induced endotoxemic male rats, injected with bacterial lipopolysacc...
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doaj-6c55b44fb6e14dd1bdb1cfc1a3fc14ee2020-11-24T23:56:00ZengBMCLipids in Health and Disease1476-511X2012-07-011119310.1186/1476-511X-11-93Bioactivity of Samsum ant (<it>Pachycondyla sennaarensis</it>) venom against lipopolysaccharides through antioxidant and upregulation of Akt1 signaling in ratsEbaid HossamAl-Khalifa MohamedIsa Ahmed MGadoa Saad<p>Abstract</p> <p>Background</p> <p>This study aimed at investigating the oxidative stress ameliorating effect, lipids profile restoration, and the anti-inflammatory effect of Samsum Ant Venom (SAV) in induced endotoxemic male rats, injected with bacterial lipopolysaccharides (LPS).</p> <p>Results</p> <p>Results revealed that LPS significantly increased the oxidative stress indications in LPS-injected rats. A significant increase of both malondialdehyde (MDA), and advanced oxidative protein products (AOPP), as well as a significant suppression of glutathione were all detected. Treatment with 100 μg/kg dose of SAV significantly restored the oxidative stress normal indications and increased the total glutathione levels. Treatment of the LPS-rats with 100 μg/kg dose of SAV showed a clear anti-inflammatory function; as the histological architecture of the hepatic tissue was partially recovered, along with a valuable decrease in the leukocytes infiltrated the hepatic tissues. Treatment of some rat groups with 600 μg/kg dose of SAV after LPS injection induced a severe endotoxemia that resulted in very high mortality rates. SAV versus the effects of LPS on AKT1, Fas, TNF-α and IFN-γ mRNA expression. SAV was found to significantly lower Fas gene expression comparing to the LPS group and restore the level of IFN-γ mRNA expression to that of the control group.</p> <p>Conclusion</p> <p>In conclusion, SAV, at the dose of 100 μg/kg body weight, maintained and restored the oxidative stability, the anti-inflammatory, and the hypolipidemic bioactivity in rats after induced disruption of these parameters by LPS injection. This improvement by SAV was mediated by upregulation of AKT1.</p> http://www.lipidworld.com/content/11/1/93AKT1Samsum ant venomOxidative stressAnti-inflammatoryLipopolysaccharides |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Ebaid Hossam Al-Khalifa Mohamed Isa Ahmed M Gadoa Saad |
spellingShingle |
Ebaid Hossam Al-Khalifa Mohamed Isa Ahmed M Gadoa Saad Bioactivity of Samsum ant (<it>Pachycondyla sennaarensis</it>) venom against lipopolysaccharides through antioxidant and upregulation of Akt1 signaling in rats Lipids in Health and Disease AKT1 Samsum ant venom Oxidative stress Anti-inflammatory Lipopolysaccharides |
author_facet |
Ebaid Hossam Al-Khalifa Mohamed Isa Ahmed M Gadoa Saad |
author_sort |
Ebaid Hossam |
title |
Bioactivity of Samsum ant (<it>Pachycondyla sennaarensis</it>) venom against lipopolysaccharides through antioxidant and upregulation of Akt1 signaling in rats |
title_short |
Bioactivity of Samsum ant (<it>Pachycondyla sennaarensis</it>) venom against lipopolysaccharides through antioxidant and upregulation of Akt1 signaling in rats |
title_full |
Bioactivity of Samsum ant (<it>Pachycondyla sennaarensis</it>) venom against lipopolysaccharides through antioxidant and upregulation of Akt1 signaling in rats |
title_fullStr |
Bioactivity of Samsum ant (<it>Pachycondyla sennaarensis</it>) venom against lipopolysaccharides through antioxidant and upregulation of Akt1 signaling in rats |
title_full_unstemmed |
Bioactivity of Samsum ant (<it>Pachycondyla sennaarensis</it>) venom against lipopolysaccharides through antioxidant and upregulation of Akt1 signaling in rats |
title_sort |
bioactivity of samsum ant (<it>pachycondyla sennaarensis</it>) venom against lipopolysaccharides through antioxidant and upregulation of akt1 signaling in rats |
publisher |
BMC |
series |
Lipids in Health and Disease |
issn |
1476-511X |
publishDate |
2012-07-01 |
description |
<p>Abstract</p> <p>Background</p> <p>This study aimed at investigating the oxidative stress ameliorating effect, lipids profile restoration, and the anti-inflammatory effect of Samsum Ant Venom (SAV) in induced endotoxemic male rats, injected with bacterial lipopolysaccharides (LPS).</p> <p>Results</p> <p>Results revealed that LPS significantly increased the oxidative stress indications in LPS-injected rats. A significant increase of both malondialdehyde (MDA), and advanced oxidative protein products (AOPP), as well as a significant suppression of glutathione were all detected. Treatment with 100 μg/kg dose of SAV significantly restored the oxidative stress normal indications and increased the total glutathione levels. Treatment of the LPS-rats with 100 μg/kg dose of SAV showed a clear anti-inflammatory function; as the histological architecture of the hepatic tissue was partially recovered, along with a valuable decrease in the leukocytes infiltrated the hepatic tissues. Treatment of some rat groups with 600 μg/kg dose of SAV after LPS injection induced a severe endotoxemia that resulted in very high mortality rates. SAV versus the effects of LPS on AKT1, Fas, TNF-α and IFN-γ mRNA expression. SAV was found to significantly lower Fas gene expression comparing to the LPS group and restore the level of IFN-γ mRNA expression to that of the control group.</p> <p>Conclusion</p> <p>In conclusion, SAV, at the dose of 100 μg/kg body weight, maintained and restored the oxidative stability, the anti-inflammatory, and the hypolipidemic bioactivity in rats after induced disruption of these parameters by LPS injection. This improvement by SAV was mediated by upregulation of AKT1.</p> |
topic |
AKT1 Samsum ant venom Oxidative stress Anti-inflammatory Lipopolysaccharides |
url |
http://www.lipidworld.com/content/11/1/93 |
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